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Cooper Laboratories

Country not established

Devices
1

What Cooper Laboratories makes

Cooper Laboratories manufactures the Vabra Abortion Unit, a surgical device designed for uterine evacuation procedures.

The Vabra Abortion Unit is classified as a Class II medical device in the US and is authorised via the FDA’s 510(k) pathway. The company is based in the United States.

AI-generated from registry data, 3 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue1

Newest first, rows 1-1 of 1

  • Vabra Abortion Unit Ref K780387

    Active Regimes: 510(k) Registry: 510(k) Class:II

Frequently asked questions

How many devices does Cooper Laboratories have in the registry?

The registry currently lists 1 device for Cooper Laboratories. Devices recorded under merged duplicate company entries are counted once.

Which registries list Cooper Laboratories's devices?

Among its 1 most recently registered device, Cooper Laboratories has devices listed in FDA 510(k) (1 device).

What risk classes do Cooper Laboratories's devices fall under?

Among its 1 most recently registered device, the classes recorded for Cooper Laboratories's devices are Class II. Each device page shows its own class and authorisation.

What are the newest devices from Cooper Laboratories in the registry?

The most recently registered devices listed for Cooper Laboratories include VABRA ABORTION UNIT.

Generated automatically from registry data and not verified by a human reviewer.